Odell Loubser

机构：BC Children's Hospital

发表论文 17 篇 · 总被引 2512 次 · h-index 11

代表论文

• Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency (1999 · Nature Genetics · 被引 1720)
• Caspase Cleavage of Mutant Huntingtin Precedes Neurodegeneration in Huntington's Disease (2002 · Journal of Neuroscience · 被引 403)
• ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels (2002 · Clinical Genetics · 被引 99)
• Mutations in ABC1 in Tangier disease and familial high-density lipoprotein (1999 · Max Planck Institute for Plasma Physics · 被引 81)
• The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery disease (2001 · Clinical Genetics · 被引 58)
• Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry (1999 · Clinical Genetics · 被引 33)